For dispensing a material with thermoplastic properties in a flowable state at an operation site in a human or animal patient, a device is used, which includes the material having thermoplastic properties in a solid state and is equipped for bringing the material into a flowable state at a distal device end positioned at the site where dispensing is desired and for driving the flowable material from this distal device end. The device comprises a rotation drive, a consumable element and a dispenser element, wherein one of the two elements is coupled to the rotation drive and wherein the consumable element comprises the material to be dispensed. The two elements are arranged with parallel longitudinal axes and the dispenser element comprises a distal end piece with a proximal face against which a distal face of the consumable element is held and advanced during dispensing.
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1. A device for dispensing a material with thermoplastic properties in a flowable state at an operation site in a human or animal patient, the device comprising:
a rotation drive,
a dispenser element comprising a shaft portion with a longitudinal axis extending from a proximal end of the shaft portion to a distal end portion which is arranged at a distal end of the shaft portion and comprises a proximal or distal face, and
a consumable element with a longitudinal axis extending from a proximal end to a distal end, at least a portion of the consumable element consisting of the material with thermoplastic properties,
wherein either the consumable element or the shaft portion is adapted to the rotation drive to be coupled thereto and the consumable element or the shaft portion is designed to be capable of transmitting the torque of the rotation drive to its distal end, and the other one of the consumable or dispenser element is adapted to be held so as to not rotate,
wherein the consumable element and the dispenser element are arranged or arrangeable with their longitudinal axes parallel to each other, and with a distal or proximal face of the consumable element in contact with the proximal or distal face of the end portion and the two faces are capable of being pressed against each other with an advancement force putting a compressive load on the consumable element along its longitudinal axis and being applied to the proximal end of the consumable element and a counter force to the distal end of the consumable element,
whereby a relative rotational movement and therewith frictional energy between the consumable element and the dispenser is creatable, which friction energy causes the material with thermoplastic properties to be transformed from the solid into the flowable state.
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13. A method for dispensing a material with thermoplastic properties in a flowable state at an operating site in a human or animal patient, the method comprising the steps of:
providing a device according to
positioning the distal end portion at the site where dispensing is desired,
applying the advancement force and the counter force and activating the rotation drive for a time sufficient for bringing material at the distal face of the consumable element into a flowable state,
whereby a relative rotational movement and therewith friction energy between the consumable element and the dispenser element is created, which friction energy causes the material with thermoplastic properties to be transformed from the solid into the flowable state,
and driving away from the end portion towards the site where dispensing is desired,
de-activating the rotation drive,
removing the distal device end from the site where dispensing is desired, thereby separating, if applicable, a dispensed portion of the material with thermoplastic properties from a rest portion of the material with thermoplastic properties which rest portion is removed with the device.
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1. Field of the Invention
The invention resides in the field of medical technology and concerns a device and a method for dispensing a material in a human or animal patient. Device and method serve for dispensing a material with thermoplastic properties in a flowable state, i.e. for bringing the material with thermoplastic properties from a solid state into a flowable state and depositing the material in the flowable state at a desired site to re-solidify. Device and method are specifically adapted for dispensing relatively small amounts of the material at an operation site in a human or animal patient but may of course also be used for dispensing the material at any other site. The device, preferably being a hand-held device, either contains the material with thermoplastic properties or is chargeable with it. The material is made flowable in a distal end portion of the device, while this distal end portion is positioned at the site where dispensing is desired.
2. Description of Related Art
Surgical processes in which materials with thermoplastic properties are liquefied in situ, are known e.g. from the publications U.S. Pat. No. 7,335,205, U.S. Pat. No. 7,008,226, WO-2005/079696, or WO-2008/034277. These publications disclose in particular methods for anchoring an implant in tissue with the aid of a material, which has thermoplastic properties and is comprised by the implant, and with the aid of vibration energy, in particular ultrasonic vibration energy. Therein the implant or part thereof is pressed against the tissue or against another implant part whereby the thermoplastic material constituting a surface of the implant or implant part is liquefied and made to penetrate the tissue where, on re-solidification, it constitutes a positive fit connection between the tissue and a portion of the thermoplastic material which was not liquefied.
The publication U.S. Pat. No. 6,620,185 discloses a device for anchoring a suture in an opening in bone tissue, wherein a material with thermoplastic properties is brought into the opening in a flowable state. The material with thermoplastic properties is stored in the dispensing device in a solid state (pellets or flexible rod to be handled like the suture), is driven to a distal device end through a cannula by pressurized air and for being dispensed is melted at this distal end, which for the melting process comprises an electric heating element, or means for inductive heating or heating with ultrasound or laser light.
It is the object of the invention to create a further device and method for dispensing a material with thermoplastic properties in a flowable state at an operation site in a human or animal patient, wherein the device and therewith the method according to the invention is to be simpler and more generally applicable than the above shortly described known device which serves the same purpose.
This object is achieved by device and method as defined in the claims.
According to an aspect of the invention, the material with thermoplastic properties is brought into the flowable state at the distal end of the device (liquefaction site) by heating a distal end of a consumable element comprising the material, wherein the named heating is effected by holding a distal face of the consumable element against a distal portion of a dispenser element and creating a relative rotational movement and therewith friction energy between the consumable element and the dispenser element. Due to this friction energy, the material of the distal end face of the consumable element becomes flowable and, due to the holding against, the flowable material flows from the interface between consumable element and dispenser element to be dispensed and the consumable element is advanced towards the interface for compensating for the dispensed material. Therein at least the force necessary for the named holding against and advancement (advancement force) and possibly the torque for effecting the rotational movement is applied to the proximal end of the consumable element. When a desired amount of the material with thermoplastic properties is dispensed, a rest of the consumable element is separated from the dispensed material by simply distancing the distal end of the device from a site where the dispensing was effected and therewith separating the dispensed part of the material with thermoplastic properties from the rest of the consumable element which remains in the device. The device according to this aspect of the invention comprises a rotation drive arranged in a proximal device region (e.g. in a housing designed for being hand held by an operator) and the dispenser element extends from the proximal device region to a distal device end. The dispenser element comprises a shaft portion and a distal end portion, wherein the end portion has a larger cross sectional area than the shaft portion and therewith a proximal face. The end portion partly closes an axially extending through opening of the shaft portion or protrudes axially from the shaft portion. The consumable element consists at least in a distal section of the material to be dispensed. The consumable element is substantially cylindrical (circular or non-circular cylinder, full or cannulated) and is arranged or arrangeable in a through opening of the shaft portion, around the shaft portion or possibly beside the shaft portion, and its distal face is in contact with the proximal face of the end portion. Either the dispenser element or the consumable element is coupled to the rotation drive for rotation around its longitudinal axis and the consumable part is held against the proximal face of the end portion by an advancement force. The advancement force is applied to the consumable element directly or indirectly by an operator or by a resilient element arranged to resiliently close a load frame in which the consumable element is put under a compressive load and the shaft portion of the dispenser element is put under a tensile load. The advancement force is transmitted through the consumable element along its full axial length.
In a variant, the liquefaction site is chosen to be at the proximal end of the consumable element. In this variant, the proximal face of the consumable element is in contact with a distal face of the end portion of the dispenser element, while the dispenser element and the consumable element are subject to a relative rotational movement. In this variant, the advancement force presses the dispenser element in the distal direction, and counter element is used to couple a counter force into the consumable element, the counter element comprising a distal end portion that has a larger cross sectional area than a shaft portion and therewith a proximal face that couples the counter force into the consumable element.
More in general, therefore, the device for dispensing a material with thermoplastic properties in a flowable state at an operation site in a human or animal patient comprises, in addition to the rotation drive, a dispenser element comprising a shaft portion with a longitudinal axis extending from a proximal end of the shaft portion to a distal end portion which is arranged at a distal end of the shaft portion and comprises a proximal or distal face. The distal end portion may have a larger cross sectional area than the shaft portion, but for the variant with the proximal liquefaction site this is not a requirement. The device further comprises a consumable element with a longitudinal axis extending from a proximal end to a distal end, at least a (distal or proximal) portion of the consumable element consisting of the material with thermoplastic properties. Either the consumable element (for example a proximal end thereof) or a proximal end of the shaft portion is adapted to the rotation drive to be coupled thereto and the consumable element or the shaft portion is designed to be capable of transmitting the torque of the rotation drive to its distal end, and the other one of the consumable or dispenser element is adapted to be held for not rotating. The consumable element and the dispenser element are arranged or arrangeable with their longitudinal axes parallel to each other, and with a distal or proximal face of the consumable element in contact with the proximal or distal face of the end portion and the two faces are capable of being pressed against each other with an advancement force putting a compressive load on the consumable element along its longitudinal axis and being applied to the proximal end of the consumable element and a counter force to the distal end of the consumable element. In many configurations, the embodiments with the liquefaction site being at the distal end of the device are preferred. One reason is that this makes possible that the material is dispensed as deeply in the tissue as possible, and (in case the tissue opening has to be made by the surgeon) it is not necessary to make a tissue opening deeper than to the site where the material is to be dispensed. A further advantage is that the assembly is potentially simpler for these embodiments.
In these embodiments, for the dispensing process, the device is firstly charged with the consumable element. Then the distal end portion of the dispenser element is positioned at a site where dispensing is desired. The advancement force is made to act on the consumable element and the rotation drive is activated to rotate the one element being coupled thereto while the other element is prevented from such rotation. Therewith there is a relative rotation between the distal face of the consumable element and the proximal face of the end portion of the dispenser element, which results in the material with thermoplastic properties at the distal end face of the consumable element to be made flowable and to flow from the liquefaction site to its immediate neighbourhood and which furthermore results in an advancement of the consumable element towards the liquefaction site. Preferably but not necessarily, the dispenser element, or the proximal face of the end portion of the dispenser element respectively, is designed for guiding the flowable material away from the liquefaction site in a predetermined (e.g. axial or radial) dispensing direction. When a desired amount of the flowable material has been dispensed, the rotation is stopped and/or the advancement force is de-activated and the distal device end is removed from the operating site.
In the described removal step, the dispensed material is separated from a part of the same material which was not made flowable and therefore, after the dispensing, remains in the device. If removal of the device from the operating site is effected immediately after or before stopping the rotation (as long as flowable material at or near the liquefaction site is not solid enough yet for forming a strong connection with the dispensed material) such removal can be effected without additional measures. If the distal end of the device is not removed until all material which has been made flowable is re-solidified, it will usually be necessary to shortly re-activate the rotation drive for weakening the connection between the dispensed material and the material at the liquefaction site, i.e. the rest of the consumable element remaining in the device, such that this connection can be broken with little effort and without destroying whatever was to be achieved with the dispensing and re-solidification of the dispensed material.
If, after one dispensing step, a rest of the consumable element remains in the device, a further dispensing step or part thereof can be effected at a different site after simple repositioning of the distal device end and in particular without any need of otherwise handling the device. If, after one or a plurality of dispensing steps, the material with thermoplastic properties present in the device is totally or nearly used up or cannot be made flowable any more for other reasons, the device is recharged by exchanging the consumable element or by adding to a rest of a first consumable element a further consumable element or part thereof.
For a given material to be dispensed, a given liquefaction site geometry, a given rotary power and a given advancement force, the amount of dispensed material is dependent on the time during which the rotation drive and the advancement force are active, or on the travel of the proximal end of the consumable element relative to the dispenser element respectively. The viscosity of the dispensed material flowing from the liquefaction site is primarily dependent on the material itself. But it is further dependent on the friction heat created at the liquefaction site (being dependent on the advancement force and on the relative rotational speed between consumable element and dispenser element) and the amount of flowable material which is made to flow from the liquefaction site by the advancing consumable element, which is again dependent on the advancement force. An increase in the named rotational speed, i.e. in the rpms of the rotation drive, will therefore tend to lower the viscosity of the dispensed material. An increase in the advancement force will tend to raise the viscosity. For automatizing the dispensing process, it therefore may be advantageous to monitor at least one of: the common activity time of rotation drive and advancement force, the travel of the proximal end of the consumable element relative to the dispenser element, rotational speed and energy consumption of the rotation drive, and the size of the advancement force. Therein set parameters are dependent on the material to be dispensed and on the liquefaction site geometry.
The device according to the invention may be a one way device which is used only as long as it contains dispensable material. However, as mentioned already further above, the device according to the invention is preferably not a one way device but is rechargeable. In this, recharging can in accordance with a first option be a recharging with the consumable element only, so that the dispenser element is re-usable. In accordance with a second option, the dispenser element may be intended for on-time use only. For example, the dispenser element may be equipped for remaining anchored, by the material with the thermoplastic properties, in the patient and thereby serve as an implant. As another example of the second option, the dispenser element may be removed after dispensing but then may be in a condition that re-using does not make sense, for example be partially covered by thermoplastic material sticking to it. In this other example, the dispensing element may be disposed of after dispensing.
Recharging of the consumable element only is particularly simple for an embodiment of the device according to the invention, in which the consumable element is cannulated for being arranged around the shaft portion of the dispenser element, in which the dispenser element is coupled to the rotation drive, and in which the consumable element is slotted over its whole length and comprises enough elasticity for being slid in a radial direction over the shaft portion. Other ways for re-charging may include decoupling of the end portion from the shaft portion and/or decoupling of the dispenser element or the consumable element from the rotation drive.
Recharging of the dispensing element and the consumable element may comprise coupling an assembly comprising the dispensing element and the consumable element to the rotation drive or coupling the dispensing element and/or the consumable element individually.
During the dispensing process, the shaft portion of the dispenser element is under a tensile load, and if coupled to the rotation drive needs to be capable of transmitting the torque from this drive to the distal device end. There is no other load put on the shaft portion and therefore the shaft portion of the dispenser element does not necessarily have to be rigid parallel to its longitudinal axis but may be flexible, as long as it is capable of withstanding the tensile load preferably without substantial axial lengthening.
The requirements of device and method according to the invention regarding the consumable element, or the material to be dispensed respectively, are very few. This means that the material can be chosen to best fit the task to be carried out. The material needs to be capable of becoming flowable at a temperature which is preferably not higher than about 350° C. In a solid state and at room or body temperature, the material needs to have mechanical properties to make it capable of transmitting the advancement force, i.e. of standing the corresponding compressive load along its axial length, without being substantially deformed by this force, in particular without substantial enlargement of its cross section. Buckling is not so relevant as it is substantially prevented by the dispenser element. Depending on the embodiment, the consumable element also needs to be capable of transmitting the torque of the rotation drive.
Experiments show that it is possible to dimension the dispenser element and the consumable element of the device according to the invention such that the distal device portion has a diameter of only a few millimeters (e.g. 4 to 8 mm) and an axial length of up to 200 mm or even more. Such dimensions render the device extremely suitable for minimal invasive surgery. Experiments also show that a rotational speeds of between approximately 10,000 and 100,000 rpm are suitable for the above named small diameter consumable elements when made of PLA. This means that rotation drives known from drilling machines as used in surgical operations or such machines themselves may be applicable in the device according to the invention, wherein it may be necessary to increase the rotational speed with the aid of a per se known gear (e.g. planetary gear) or to adapt a coupling means (e.g. chuck) for coupling one of the device elements to the rotation drive.
In all embodiments, optionally in addition to the rotational movement, auxiliary means may be used to help bring the distal (or proximal) face of the consumable element into a flowable state. An example of such an auxiliary means is a heater that for example locally introduces heat into the dispenser element in a vicinity of the proximal or distal face.
The device according to the invention is applicable in substantially all surgical procedures in which a material with thermoplastic properties is a suitable material and is needed in a specific place of an operation site where the material cannot be introduced in a solid state or cannot take over the intended function (e.g. positive fit) if brought in a solid state. Exemplary such surgical procedures are fixation of a suture or wire in a tissue opening, application of spacing material between an endoprosthesis and tissue, introduction of blocking or adhesive material between tissue parts, between tissue and an implanted element or between implanted elements, in-situ forming of anchor pins for fixation of bone plates (e.g. for osteosynthesis), rods (e.g. for spinal fixation), endoprostheses for joint resurfacing, webs or membranes on tissue, augmentation of tissue, in particular of cancellous bone, filling of small tissue defects, repair of endoprosthesis fixation made of bone cement, sealing of cavities as e.g. in tubular bones or dental roots.
A special class of applications of the device according to the invention are applications in which the dispenser element is left where it was positioned for the dispensing process, e.g. in a tissue opening, where it constitutes an implant being anchored in the tissue of bottom and/or walls of the tissue opening. In such embodiments, the dispenser element may comprise an additional functional structure that serves a further purpose. For example, it may comprise one or a combination of:
a securing structure, for example at its proximal end, that serves for a further element to be coupled to the dispenser element (that is an implant) and/or to the tissue in which the dispenser element is anchored;
self-reaming and/or cutting structures that are to create and/or enlarge the tissue opening when the dispenser element is first introduced (Examples of such structures are a self-cutting blade or a tapping thread or the structures taught in WO 2005/079696, incorporated herein by reference. Especially, in the embodiments of WO 2005/079696 that comprise a cannulated solid structure with openings for the thermoplastic material, the taught cannulated solid structure may serve as dispensing element in accordance with the teaching of the present application.);
additional anchoring structures, such as a thread, as for example taught, referring to a pedicle screw in U.S. provisional patent application No. 61/259,383 incorporated herein by reference;
additional functional structures in contact with the tissue, as for example taught in WO 2004/017 857 incorporated herein by reference. Especially, in the embodiments of WO 2004/017 857 that comprise a cannulated solid structure with openings for the thermoplastic material, the taught cannulated solid structure may serve as dispensing element in accordance with the teaching of the present application. An example of additional functional structures are surface regions that are structured to advance osseointegration, for example by having an appropriate coating and/or an appropriate surface roughness. Another example of an additional functional structure is drug delivery structures. Further functional structures of implants, which functional structures are either in contact with the tissue in which the implant is anchored or protrude from this tissue, can be found in U.S. Pat. No. 7,335,205, incorporated herein by reference in its entirety.
A first example of a securing structure is a securing collar or head. For example, if the dispenser element is cannulated (i.e. with an axial opening/cannulation open to the proximal side) with at least one bore through which the thermoplastic material may flow out of the cannulation and into tissue openings and/or other structures, the cannulated portion (cannulated shaft portion) may comprise a proximal outward-extending collar. Such a collar then may be used to secure a further element—such as a plate—against the tissue, when such further element has a through opening with an inner diameter approximately corresponding to the outer diameter of the cannulated portion.
As an alternative or in addition to comprising a collar as the securing structure, other structures also may be present, such as a proximal interior or exterior thread, a post, a feature of a snap-on or bayonet coupling, a rod guiding structure etc.
For example, if the dispenser element is to serve as a dental implant, an interior thread open to the proximal side may serve for securing a basal screw. If the dispenser element is to serve as a dental implant and comprises a post as a securing structure such post may serve for securing a dental crown or dental prosthesis.
As another example, if the dispenser element is to serve as a pedicle screw, it may comprise proximal bolt guiding and/or plate guiding structures for being secured to a spine stabilizing bolt and/or plate or the like.
A cannulated dispenser element serving as an implant element may in many situations be used to replace a classical bone screw with a screw head. Also, when serving as a bone screw replacement, it may, in addition to comprising the mentioned openings, optionally further comprise additional functional structures such as an outer thread, a reaming structure etc.
In addition or as an alternative to replacing a bone screw, the dispenser element may, together with the dispensed material, function in a blind-rivet-like manner. This is if there is no or not enough sufficiently firm tissue at the site where the thermoplastic material is dispensed, anchoring may be achieved by dispensing underneath a layer of firm tissue.
In embodiments, the openings may be positioned to ensure sub-cortical anchoring of the dispenser element. Generally, a sub-cortical anchoring may, for example, be obtained if a distance between an outer surface of the bone tissue and the proximal end of an opening through which the thermoplastic material exits from the cannulation is for example between 2 mm and 7 mm, especially between 3.5 mm and 5.5 mm (this being quantities that hold for grown-up persons). Accordingly, a distance between a distal end face of a further device resting against the bone tissue (such as a fixation device body of a spine stabilization device) and the proximal onset of the opening can be chosen to be of the same order, i.e. between 2 mm and 7 mm, especially between 3.5 mm and 5.5 mm. Also in embodiments for sub-cortical anchoring, the dispenser element may comprise portions that are substantially distally of the opening(s)—in these embodiments, therefore, the end portion may be elongate, and its axial extension may even be comparable to the axial extension of the shaft portion. Examples of outer geometries of dispenser elements may, for example, be found in FIG. 33 or 42 of PCT/CH2010/000045 incorporated herein by reference. Compared to the embodiment of FIG. 43 of PCT/CH2010/000045, the proximal face of the end portion of the element is, for serving as dispenser element according to the present teaching, adapted to allow a relative rotational movement of the consumable element and the dispenser element.
In other applications, the dispenser element is of the kind where the end portion protrudes radially from the shaft portion, with the consumable element, for example, comprising an axial through opening. In embodiments where the dispenser element is to remain anchored in the tissue, the shaft portion may comprise a securing structure, such as a thread and thereafter serve as anchor for a further device, such as a stabilizing device.
A further group of applications concerns augmentation. In such applications, the dispenser element is in most embodiments removed from the tissue after the dispensing process. For example, for augmentation the dispenser element may again be of the cannulated kind. It may be introduced in a tissue opening so that the opening/openings through which the thermoplastic material exits is in vicinity to brittle and/or weak tissue to interpenetrate such tissue. In addition, the dispenser element in such embodiments may serve as a profile body, for example defining the shape of an inner thread of the tissue opening. The function of such a profile body is described for example in U.S. provisional patent application No. 61/259,383 incorporated herein by reference in its entirety. Compared to embodiments of, for example, FIGS. 1-7 of U.S. 61/259,383, the proximal face of the end portion of the element is, for serving as dispenser element according to the present teaching, adapted to allow a relative rotational movement of the consumable element and the dispenser element. The following materials are capable of being dispensed with the aid of the device according to the invention wherein the named materials are, in particular, suitable for dispensing the material in order to establish a load-bearing connection between two tissue parts, between a tissue part and an implanted item or between two implanted items:
resorbable polymers such as polymers based on lactic and/or glycolic acid (PLA, PLLA, PGA, PLGA etc.) or polyhydroxy alkanoates (PHA), polycaprolactone (PCL), polysaccharides, polydioxanes (PD) polyanhydrides, polypeptides or corresponding copolymers or composite materials containing the named polymers as a component; or non-resorbable polymers such as polyolefines (e.g. polyethylene), polyacrylates, polymethacrylates, polycarbonates, polyamides, polyester, polyurethanes, polysulfones, polyarylketones, polyimides, polyphenylsulfides or liquid crystal polymers LCPs, polyacetales, halogenated polymers, in particular halogenated polyolefines, polyphenylenesulfides, polysulfones, polyethers or equivalent copolymers or composite materials containing the named polymers as a component. Specific embodiments of degradable materials are Polylactides like LR706 PLDLLA 70/30, R208 PLDLA 50/50, L210S, and PLLA 100% L, all of Böhringer. A list of suitable degradable polymer materials can also be found in: Erich Wintermantel und Suk-Woo Haa, “Medizinaltechnik mit biokompatiblen Materialien und Verfahren”, 3. Auflage, Springer, Berlin 2002 (in the following referred to as “Wintermantel”), page 200; for information on PGA and PLA see pages 202 ff., on PCL see page 207, on PHB/PHV copolymers page 206; on polydioxanone PDS page 209. Discussion of a further bioresorbable material can for example be found in C A Bailey et al., J Hand Surg [Br] 2006 April; 31(2):208-12.
Non-resorbable materials such as polyetherketone (PEEK Optima, Grades 450 and 150, Invibio Ltd), Polyetherimide, Polyamide 12, Polyamide 11, Polyamide 6, Polyamide 66, Polycarbonate, Polymethylmethacrylate, Polyoxymethylene. An overview table of polymers and applications is listed in Wintermantel, page 150; specific examples can be found in Wintermantel page 161 ff. (PE, Hostalen Gur 812, Höchst AG), pages 164 ff. (PET) 169ff. (PA, namely PA 6 and PA 66), 171 ff. (PTFE), 173 ff. (PMMA), 180 (PUR, see table), 186 ff. (PEEK), 189 ff. (PSU), 191 ff (POM—Polyacetal, tradenames Delrin, Tenac, has also been used in endoprostheses by Protec). A further suitable group of polymers are Polycarbonate Urethanes, such as, for example the products sold under the trade name “Bionate®” by DSM Biomedical, especially products with a hardness of between 55 shore D and 75 shore D, especially the hardness grades 55D, 65D, and 75D.
The materials to be dispensed may contain foreign phases or compounds serving further functions. In particular, a thermoplastic base material may be strengthened by admixed fibers or whiskers (e.g. of calcium phosphate ceramics or glasses) and such represent a composite material. The thermoplastic material may further contain components which expand or dissolve (create pores) in situ (e.g. polyesters, polysaccharides, hydrogels, sodium phosphates) or compounds to be released in situ and having a therapeutic effect, e.g. promotion of healing and regeneration (e.g. growth factors, antibiotics, inflammation inhibitors or buffers such as sodium phosphate or calcium carbonate against adverse effects of acidic decomposition). If the thermoplastic material is resorbable, release of such compounds is delayed.
Fillers used may include degradable, osseostimulative fillers to be used in degradable polymers, including: β-Tricalciumphosphate (TCP), Hydroxyapatite (HA, <90% crystallinity; or mixtures of TCP, HA, DHCP, Bioglasses (see Wintermantel).
Osseo-integration stimulating fillers that are only partially or hardly degradable, for non degradable polymers include: Bioglasses, Hydroxyapatite (>90% cristyllinity), HAPEX®, see S M Rea et al., J Mater Sci Mater Med. 2004 September; 15(9):997-1005; for hydroxyapatite see also L. Fang et al., Biomaterials 2006 July; 27(20):3701-7, M. Huang et al., J Mater Sci Mater Med 2003 July; 14(7):655-60, and W. Bonfield and E. Tanner, Materials World 1997 January; 5 no. 1:18-20.
Embodiments of bioactive fillers and their discussion can for example be found in X. Huang and X. Miao, J Biomater App. 2007 April; 21(4):351-74), J A Juhasz et al. Biomaterials, 2004 March; 25(6):949-55.
Particulate filler types include: coarse type: 5-20 μm (contents, preferentially 10-25% by volume), sub-micron (nanofillers as from precipitation, preferentially plate like aspect ratio>10, 10-50 nm, contents 0.5 to 5% by volume).
A few exemplary embodiments of the device according to the invention are described in detail in connection with the following Figs., wherein:
The distal end portion 6.2 of the dispenser element closes the cannulated shaft portion only partly, i.e. it comprises openings 6.3 e.g. bores extending in an axial to radial direction or it consist of or comprises a material comprising an open porosity (e.g. sintered metal or ceramic material or metal foam) and being suitable for transfer of the flowable material from the inside of the dispenser element to the surroundings thereof. The end portion 6.2 may be arranged on the shaft portion 6.1 to be removable (e.g. threaded or snapped on) or not removable (e.g. integral part of shaft portion or welded thereto). The through opening of the shaft portion 6.1 is dimensioned such that rotation of the consumable element 4 causes no, or only very little, lateral friction. For keeping the consumable element and the shaft portion in coaxial alignment, a bearing 7 (preferably bush bearing) may be arranged in a proximal region of the dispenser element.
For a dispensing process, the consumable element 5 is coupled to the rotation drive, introduced in the dispenser element 6 with its distal face facing the proximal face of the end portion 6.2 of the dispenser element 6. For a fully manual dispensing process, it is an operator who holds the housing 2, forces it in a direction towards the dispenser element 6 (advancement force) and activates the rotation drive. At the same time he holds the dispenser element 6 by its proximal end for counteracting the advancement force and for preventing the dispenser element 6 from rotating. For this holding the dispenser element 6 may comprise a proximal flange 6.4 or other radial protrusion. Part of the named functions of the operator may be taken over by a tissue surface against which the flange 6.4 of the end portion 6.2 is pressed by the advancement force. When the rotation drive 1 and the advancement force are active, the distal face of the consumable element 5 is rotated relative to the end portion 6.2 of the dispenser element 6 such causing friction and heating of the material with thermoplastic properties which thereby is made flowable, and by the advancement force is driven through the openings 6.3 of the end portion 6.2 of the dispenser element 6 to be dispensed at a site on the outside thereof.
The above described operator actions regarding holding the dispenser element 6 and pressing the housing 1 against it can also be achieved with a resilient element 8 (e.g. spring) which is mounted between the proximal end of the dispenser element 6 (e.g. flange 6.4) and the housing 2 such that it pulls these towards each other. It may be possible also that the resilient element 8 functions as a centering element in addition to bearing 7 or in the place of it.
The openings 6.3 of the end portion of the dispenser element can be adapted to guide the flowable material in a specific direction. This direction may be e.g. an axial direction, a plurality of radial directions regularly spread around the circumference of the dispenser element 6, one specific radial direction, a plurality of specific radial directions, or a direction or directions which are combinations of the named directions.
The dispenser element 6 being a part of the device according to the invention is in some embodiments removed together with the rest of the consumable element 5 and the rotation drive 1 in housing 2. In particular, in the case of the operator handling the device which does not comprise the resilient element 8 (dispenser element 6 possibly not connected to any of the other device parts) or in which the connection between a resilient element and the dispenser element is releasable, the dispenser element 6 may easily be left where it was positioned for the dispensing process, e.g. in a tissue opening, where it constitutes an implant being anchored in the tissue of bottom and/or walls of the tissue opening. In this case, the dispenser element may be part of a larger implant and therefore have a form which is dictated by the implant function.
As can be seen from
In particular, if the material to be dispensed becomes flowable only in a relatively high temperature range, it may be advantageous to make the dispenser element 6 of a heat insulating material (e.g. thermoset polymer or ceramic material) such that the thermal load put on the tissue at the site of dispensing is reduced to only the heat energy of the flowable material.
As, in the first embodiment of the device according to the invention, the rotating consumable element 5 is sheltered from contact with tissue by the dispenser element 6 and therefore cannot damage tissue, this embodiment is particularly suitable for dispensing processes at the bottom of narrow tissue openings in which contact between the distal device portion and the tissue, other than where dispensing is desired, can hardly be fully prevented.
For recharging the device according to
In embodiments where sheltering of tissue from rotational movement is not a requirement, the embodiment of
The first embodiment of the device according to the invention as shown in
The resilient element 8 is mounted between the proximal end of the dispenser element 6 and the rotation drive 1 or a proximal portion of the consumable element 5.
The shaft portion 6.1 and/or the end portion 6.2 of the dispenser element 6 is at least partly not rigid but flexible (wire, rope, membrane, web, non-woven etc.).
The rotation drive comprises an angular gear or bevel gear to enable the distal device portion to be angled relative to the rotation axis of the rotation drive.
Instead of the consumable element 5, the dispenser element 6 is coupled to the rotation drive 1 (e.g. cannulated drilling machine) and the consumable element 5 is held to prevent it from rotating.
The elements of the device according to
The material of the distal end of the consumable element 5, which is the material with thermoplastic properties and is to be dispensed, is made flowable through friction heat created between the proximal face of the end portion 6.2 of the dispenser element 6 and the distal face of the consumable element 5 by rotation of the dispenser element 6. For effecting the friction and the advancement of the proximal end of the consumable element 5, an operator holds e.g. the housing 2 and pushes the proximal end of the consumable element 5 against the end portion 6.2, for which purpose the proximal end of the consumable element 5 may comprise a flange 5.5 or other radial protrusion. The same is achieved by mounting a resilient element 8 between the proximal end of the consumable element 5 and the housing 2, the rotation drive 1, or a proximal portion of the shaft portion 6.1, wherein the resilient element 8 is biased to push the named elements away from each other such forming a load frame in which the consumable element 5 is put under a compressive load and the shaft portion 6.1 of the dispenser element 6 is put under a tensile load.
Again a proximal portion of the consumable element 5 may not consist of the material to be dispensed wherein there is no need for the different portions of the consumable element 5 to be connected with each other.
For re-charging the device according to
The device according to
The resilient element 8 is mounted between the proximal end of the consumable element 5 and the rotation drive 1 or a proximal portion of the dispenser element 6.
A proximal end of the shaft portion 6.1 of the dispenser element 6 is a flexible rod or rope guided in a flexible cannula and allowing a freely selectable angle between the rotation axis of the rotation drive 1 and the longitudinal axis of the consumable element 5.
The consumable element is coupled to the rotation drive (e.g. cannulated drilling machine) and the dispenser element is held for counteracting the advancement force and for preventing the consumable element from rotating with the dispenser element.
Yet a further variant of the device according to
In many embodiments, the interface between the end portion 6.2 of the dispenser element 6 and the consumable element 5 will be held at a constant position in vicinity of the opening 11.1. Therefore, in these embodiments, the consumable element will be subject to a forward movement (a movement into the distal direction) when being consumed. To this end, in accordance with a first option the consumable element will be designed to protrude substantially from the proximal end face of the protective sheath 11 so that it can be pushed further into the sheath during the dispensing process. In accordance with a second option, the device further comprises a pusher 15 adapted to engage into the elongate cavity and to push the consumable element further to the distal side when it gets shorter while being consumed. In the depicted configuration, the pusher 15 comprises a shaft portion 15.1 with an outer diameter adapted to the inner diameter of the elongate cavity. The resilient element 8—if present—may then be arranged between the housing 2 and a flange 15.2 of the pusher to push the same to the distal direction. An outer support not depicted in
An additional bearing or additional bearings 17.1, 17.2 may be present between the protective sheath 11 and the consumable element 5 to guide the latter in the elongate cavity; since the consumable element 5 is not to rotate the bearings optionally by rotationally asymmetric and engage into structures (such as longitudinal trenches) of the consumable element to prevent their rotational movement. In addition or as an alternative, the elongate cavity may be rotationally asymmetric with the consumable element outer shape adapted thereto, the consumable element being slidingly inserted.
In the embodiment of
Of course, also in the embodiment of
In addition to the friction heat created by the relative rotation between consumable element and dispenser element, it is possible to apply further heating energy to the consumable element in the area of its distal face for furthering the liquefaction process. Such further heating energy may be constituted by resistively or inductively heating the end portion of the dispenser element or in particular by adsorbing electromagnetic radiation, e.g. laser light in this end portion, wherein the laser light is preferably coupled into the proximal end of the consumable element and is guided through the consumable element to be absorbed in the end portion of the dispenser element.
The concept of the variant of
Mock, Elmar, Mayer, Jörg, Weber, Urs
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Jan 10 2012 | MAYER, JORG | WOODWELDING AG | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 027621 | /0580 | |
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